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Wdr89m1Anu
Chemically induced Allele Detail
Summary
Symbol: Wdr89m1Anu
Name: WD repeat domain 89; mutation 1, Australian National University
MGI ID: MGI:5563398
Synonyms: ENU26:029:WDR89
Gene: Wdr89  Location: Chr12:75677370-75716311 bp, - strand  Genetic Position: Chr12, 32.89 cM, cytoband D1
Alliance: Wdr89m1Anu page
Mutation
origin
Strain of Origin:  C57BL/6NCrlAnu
Project Collection: APF ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a A to T point mutation at position 524 on cDNA (ENSMUST00000062370) in exon 2 and results in the amino acid substitution of Leucine to STOP at position 143. (J:104190)
Inheritance:    Recessive
Phenotypes
Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Allelic Composition
Genetic Background
Cell Line(s)
 
Phenotypes:
Affected Systems
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immune system
N
immune system phenotype
N
View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Wdr89 Mutation:  65 strains or lines available
References
Original:  J:104190 The Australian Phenomics Facility at The Australian National University, Heritable mouse mutants from the ENU mutagenesis program at the Australian Phenomics Facility at The Australian National University. MGI Direct Data Submission. 2006-2014;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory

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